15 ott - Fiumicino
Barrington James
I am looking to connect with freelance clinical research associates who have experience in the monitoring of cardiovascular + medical device studies. You will be taking ownership of monitoring a single site, joining an already established team based out of Rome Italy, on a 12-month tempo parziale contract. Key responsibilities: * Experience CRA with expertise in monitoring medical device clinical studies. * Conduct Source Data Verification and Source Data Review, ensuring data accuracy, and consistency with the EDC system. * Ensure compliance with study protocols, ICH-GCP guidelines, and applicable Italian regulatory requirements. * Manage and reconcile Trial Master File and Investigator Site File documentation to ensure accurate and complete site-level records. Key requirements: * Fluent in Italian and with professional working proficiency in English.
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